Department of Gastroenterology, University Hospitals Leuven, KU Leuven-University of Leuven, Leuven, Belgium.
Department of Pharmaceutical and Pharmacological Sciences, Laboratory for Therapeutic and Diagnostic Antibodies, KU Leuven-University of Leuven, Leuven, Belgium.
Clin Gastroenterol Hepatol. 2015 Mar;13(3):531-8. doi: 10.1016/j.cgh.2014.07.055. Epub 2014 Aug 10.
BACKGROUND & AIMS: Infliximab is effective for patients with refractory ulcerative colitis (UC), but few factors have been identified that predict long-term outcome of therapy. We aimed to identify a panel of markers associated with outcome of infliximab therapy to help physicians make personalized treatment decisions.
We collected data from the first 285 patients with refractory UC (41% female; median age, 39 y) treated with infliximab before July 2012 at University Hospitals Leuven, in Belgium. We performed a Cox regression analysis to identify independent factors that predicted relapse-free and colectomy-free survival, and used these factors to create a panel of markers (risk panel).
During a median follow-up period of 5 years, 61% of patients relapsed and 20% required colectomy. Independent predictors of relapse-free survival included short-term complete clinical response (odds ratio [OR], 3.75; 95% confidence interval [CI], 2.35-5.97; P < .001), mucosal healing (OR, 1.87; 95% CI, 1.17-2.98; P = .009), and absence of atypical perinuclear antineutrophil cytoplasmic antibodies (pANCA) (OR, 1.96; 95% CI, 1.23-3.12; P = .005). Independent predictors of colectomy-free survival included short-term clinical response (OR, 7.74; 95% CI, 2.76-21.68; P < .001), mucosal healing (OR, 4.02; 95% CI, 1.16-13.97; P = .028), baseline level of C-reactive protein (CRP) of 5 mg/L or less (OR, 2.95; 95% CI, 1.26-6.89; P = .012), and baseline level of albumin of 35 g/L or greater (OR, 3.03; 95% CI, 1.12-8.22; P = .029). Based on serologic analysis of a subgroup of 112 patients, levels of infliximab greater than 2.5 μg/mL at week 14 of treatment predicted relapse-free survival (P < .001) and colectomy-free survival (P = .034). A risk panel that included levels of pANCA, CRP, albumin, clinical response, and mucosal healing identified patients at risk for UC relapse or colectomy (both P < .001).
Clinical response and mucosal healing were confirmed as independent predictors of long-term outcome from infliximab therapy in patients with UC. We identified additional factors (levels of pANCA, CRP, and albumin) to create a risk panel that predicts long-term outcomes of therapy. Serum levels of infliximab at week 14 of treatment also were associated with patient outcomes. Our risk panel and short-term serum levels of infliximab therefore might be used to guide therapy.
英夫利昔单抗对难治性溃疡性结肠炎(UC)患者有效,但目前尚识别出可预测治疗长期结局的少数因素。我们旨在确定与英夫利昔单抗治疗结局相关的标志物组合,以帮助医生做出个体化的治疗决策。
我们收集了比利时鲁汶大学医院 2012 年 7 月前接受英夫利昔单抗治疗的 285 例难治性 UC 患者(41%为女性;中位年龄为 39 岁)的数据。我们进行了 Cox 回归分析,以确定预测无复发和无结肠切除生存的独立因素,并使用这些因素创建了标志物组合(风险组合)。
在中位随访 5 年期间,61%的患者复发,20%需要结肠切除。无复发生存的独立预测因素包括短期完全临床缓解(比值比[OR],3.75;95%置信区间[CI],2.35-5.97;P<0.001)、黏膜愈合(OR,1.87;95%CI,1.17-2.98;P=0.009)和缺乏非典型核周抗中性粒细胞胞质抗体(pANCA)(OR,1.96;95%CI,1.23-3.12;P=0.005)。无结肠切除生存的独立预测因素包括短期临床缓解(OR,7.74;95%CI,2.76-21.68;P<0.001)、黏膜愈合(OR,4.02;95%CI,1.16-13.97;P=0.028)、基线 C 反应蛋白(CRP)水平为 5mg/L 或更低(OR,2.95;95%CI,1.26-6.89;P=0.012)和基线白蛋白水平为 35g/L 或更高(OR,3.03;95%CI,1.12-8.22;P=0.029)。基于 112 例患者的血清学分析亚组,治疗第 14 周时英夫利昔单抗水平大于 2.5μg/mL 预测无复发生存(P<0.001)和无结肠切除生存(P=0.034)。包括 pANCA、CRP、白蛋白、临床反应和黏膜愈合在内的风险组合确定了具有 UC 复发或结肠切除风险的患者(均 P<0.001)。
临床反应和黏膜愈合被确认为 UC 患者接受英夫利昔单抗治疗长期结局的独立预测因素。我们确定了其他因素(pANCA、CRP 和白蛋白水平)来创建预测治疗长期结局的风险组合。治疗第 14 周时的血清英夫利昔单抗水平也与患者结局相关。因此,我们的风险组合和英夫利昔单抗的短期血清水平可能用于指导治疗。